Literature DB >> 1750330

Recurrent corneal epithelial erosions in Alport's syndrome.

J P Burke1, L G Clearkin, J F Talbot.   

Abstract

Alport's syndrome is a heritable disorder of uncertain aetiology characterized by nephritis, sensorineural deafness and ocular abnormalities. Bilateral corneal epithelial erosions are a previously unreported finding which support the hypothesis that Alport's syndrome is a disorder of selected basement membranes.

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Mesh：

Year:  1991        PMID： 1750330     DOI： 10.1111/j.1755-3768.1991.tb02041.x

Source DB:  PubMed          Journal:  Acta Ophthalmol (Copenh)        ISSN： 0001-639X


  4 in total

Review 1.  Ocular features in Alport syndrome: pathogenesis and clinical significance.

Authors:  Judy Savige; Shivanand Sheth; Anita Leys; Anjali Nicholson; Heather G Mack; Deb Colville
Journal:  Clin J Am Soc Nephrol       Date:  2015-02-03       Impact factor: 8.237

2.  Temporal macular thinning associated with X-linked Alport syndrome.

Authors:  Faisal Ahmed; Kandon K Kamae; Denise J Jones; Margaret M Deangelis; Gregory S Hageman; Martin C Gregory; Paul S Bernstein
Journal:  JAMA Ophthalmol       Date:  2013-06       Impact factor: 7.389

3.  Maculopathy, Fundus Changes and Anterior Lenticonus in Alport Syndrome.

Authors:  Mirko Ratkovic; Ajla Pidro; Aida Pidro
Journal:  Beyoglu Eye J       Date:  2021-02-11

4.  Characterization of Choriocapillaris and Choroidal Abnormalities in Alport Syndrome.

Authors:  Maria Vittoria Cicinelli; Markus Ritter; Hassan Tausif; Cybele Ghossein; Constantin Aschauer; Franco Laccone; Mato Nagel; Lee M Jampol; Manjot K Gill
Journal:  Transl Vis Sci Technol       Date:  2022-03-02       Impact factor: 3.283
  4 in total

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